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dbVar

Database of genomic structural variation

nsv6130971

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:mobile element insertion
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:62

Description:nsv5561772 from Byrska-Bishop et. al 2021. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 193 SVs from 45 studies. See in: genome view

Remapped(Score: Perfect):22,741,752-22,741,813

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6130971	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	22,741,752	22,741,813
nsv6130971	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	22,924,554	22,924,615

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17966467	mobile element insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17966467	Remapped	Perfect	NC_000019.10:g.227 41752_22741813ins?	GRCh38.p12	First Pass	NC_000019.10	Chr19	22,741,752	22,741,813
nssv17966467	Submitted genomic		NC_000019.9:g.2292 4554_22924615ins?	GRCh37 (hg19)		NC_000019.9	Chr19	22,924,554	22,924,615

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17966467	0.135	743	5486

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